Bisoprolol Fumarate Tablet
Product Images NDC 70954-456

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Bisoprolol Fumarate (NDC 70954-456). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novitium Pharma Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Biso-structure (Biso Structure)

Chemical structure of Bisoprolol Fumarate, showing the bisoprolol molecule with attached functional groups and the fumarate component, represented in a typical structural formula format.*

FDA Label Image

Biso-10mg-100 (Bisoprolol 10mg 100)

Label for Bisoprolol Fumarate Tablets USP 10 mg oral tablets by Novitium Pharma LLC. The label highlights 100 tablets per container with storage instructions (20° to 25°C). It includes the NDC 70954-456-20 and a barcode. The label states the product is Rx only and gives manufacturing details.*

FDA Label Image

Biso-10mg-30 (Bisoprolol 10mg 30)

Label for Bisoprolol Fumarate Tablets USP 10 mg by Novitium Pharma LLC. The label indicates a unit-of-use packaging containing 30 tablets. It includes storage instructions at controlled room temperature and a barcode. The label also states 'Rx only' and provides manufacturer address details.*

FDA Label Image

Biso-5mg-100 (Bisoprolol 5mg 100)

Label for Bisoprolol Fumarate Tablets, USP 5 mg, manufactured by Novitium Pharma LLC. The label indicates 100 tablets in the package. It includes dosage strength, storage instructions (20° to 25°C), and general handling warnings. The label features the Novitium Pharma logo and a barcode on the right.*

FDA Label Image

Biso-5mg-30 (Bisoprolol 5mg 30)

Label for Bisoprolol Fumarate Tablets, USP 5 mg, a prescription oral tablet manufactured by Novitium Pharma LLC. The label includes dosage strength, NDC 70954-455-10, quantity of 30 tablets, storage instructions, and manufacturer address in New Jersey.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.